drugset / Trial / NCT02345252

Switch Study to Evaluate the Safety and Efficacy of Emtricitabine/Rilpivirine/Tenofovir Alafenamide (FTC/RPV/TAF) Fixed Dose Combination (FDC) in HIV-1 Positive Adults Who Are Virologically Suppressed on Emtricitabine/Rilpivirine/Tenofovir Disoproxil Fumarate (FTC/RPV/TDF)

NCT02345252

Phase 3 Completed 632 enrolled Gilead Sciences
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to evaluate the noninferiority of switching to emtricitabine/rilpivirine /tenofovir alafenamide (FTC/RPV/TAF) fixed-dose combination (FDC) as compared to continuing FTC/RPV/tenofovir disoproxil fumarate (TDF) FDC (FTC/RPV/TDF) in virologically suppressed HIV-1 infected participants.

Timeline

Start
2015-01-26
Primary completion
2016-06-22
Completion
2019-01-09

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject FTC/RPV/TAF Unknown 25 mg Oral
Comparator Tenofovir disoproxil fumarate Small molecule 300 mg Oral
Background Rilpivirine Small molecule 25 mg Oral
Background emtricitabine Other / unclassified 200 mg Oral